| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:74291871-74292255 | Common:3; Rare:111 | ||||
| chr18:74496066-74496421 | Common:4; Rare:114 | ||||
| chr18:74597601-74597914 | Common:2; Rare:83 | ||||
| chr18:75208500-75208631 | Common:2; Rare:34 | ||||
| chr18:79988367-79988671 | Common:4; Rare:114; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:572252-572637 | Common:3; Rare:193 | ||||
| chr19:633520-633759 | Common:8; Rare:106 | ||||
| chr19:663147-663445 | Common:2; Rare:122 | ||||
| chr19:821914-822077 | Rare:39 | ||||
| chr19:893167-893484 | Common:3; Rare:132 | ||||
| chr19:913173-913264 | Rare:27 | ||||
| chr19:984230-984356 | Rare:44 | ||||
| chr19:1269098-1269346 | Common:2; Rare:90 | ||||
| chr19:1354793-1355003 | Rare:87 | ||||
| chr19:1446166-1446323 | Rare:43 |